0
Study |

Spitz Tumors in Children:  A Grading System for Risk Stratification FREE

Alain Spatz, MD; Eduardo Calonje, MD; Susan Handfield-Jones, MD; Raymond L. Barnhill, MD
[+] Author Affiliations

From the Department of Pathology, Institut Gustave-Roussy, Villejuif, France (Dr Spatz); St John's Institute of Dermatology, St Thomas' Hospital, London, England (Drs Calonje and Handfield-Jones); and Division of Dermatopathology and Oral Pathology, the Johns Hopkins Medical Institutions, Baltimore, Md (Dr Barnhill).


Arch Dermatol. 1999;135(3):282-285. doi:10.1001/archderm.135.3.282.
Text Size: A A A
Published online

Objective  To describe a grading system for risk stratification of atypical Spitz tumors in children and adolescents. In some circumstances, unequivocal distinction between Spitz nevus and melanoma is practically impossible. It is likely that these lesions for which we lack specific diagnostic criteria represent a broad histological continuum extending from benign to malignant tumors. Therefore, we propose that Spitz tumors be categorized into low-, intermediate-, or high-risk categories based on the accumulation of abnormal features.

Design  Retrospective study.

Settings  Institutional practice.

Patients  We present 30 cases of atypical Spitz tumors in patients younger than 18 years evaluated for at least 3 years or in whom a metastatic event developed during this period.

Intervention  None.

Main Outcome Measure  The grading system was formulated after data collection.

Results  Among the parameters studied, only diagnosis at age greater than 10 years, diameter of the lesion greater than 10 mm, presence of ulceration, involvement of the subcutaneous fat (level V), and mitotic activity of at least 6/mm2 carried a likelihood ratio greater than 1.50 and were therefore used for the grading system.

Conclusion  The application of an objective grading system, such as the one described herein for the first time, is the first step in providing useful information for the management of atypical Spitz tumors.

Figures in this Article

THE TYPICAL Spitz nevus is a benign tumor that can be distinguished from melanoma in most instances. However, as stated by Allen and Spitz1 in 1953, in some circumstances, unequivocal distinction between Spitz nevus and melanoma is practically impossible. It is likely that these lesions for which we lack specific diagnostic criteria represent a broad histological continuum extending from benign to malignant tumors. Therefore, we propose that Spitz tumors be categorized into low-, intermediate-, or high-risk categories based on the accumulation of abnormal features. We describe a scoring system based on data from a series of 30 patients aged 17 years or younger who presented with an atypical Spitz tumor.

DESIGN

The 30 patients with a histopathologic diagnosis of atypical Spitz tumor whose data formed the basis of the scoring system were less than 18 years of age when the diagnosis of atypical Spitz tumor was made, were evaluated for at least 3 years or developed a metastatic event during this period, and had representative slides available for review. The cases were collected from 1959 through 1997, the range of earliest and latest reports. The slides came from the regular or consultation files of the following institutions: Institut Gustave-Roussy, Villejuif, France; St John's Institute of Dermatology at St Thomas' Hospital, London, England; Children's Hospital and Brigham and Women's Hospital, Boston, Mass; and the Johns Hopkins Medical Institutions, Baltimore, Md. Twenty-six cases had been previously reported, including 8 cases from Institut Gustave-Roussy,2 11 cases from St Thomas' Hospital,3 and 7 cases from Children's Hospital, Brigham and Women's Hospital, and the Johns Hopkins Medical Institutions.4 The term atypical Spitz tumor was used in this study to designate lesions sharing some but not all of the classic features of Spitz nevi or displaying unusual features.46 These features are summarized in Table 1.

Table Graphic Jump LocationTable 1. Comparison of Classic Spitz Nevi and Atypical Spitz Tumors*
CLINICAL PARAMETERS

Clinical variables included age at diagnosis (≤10 vs >10 years), sex, lesion site (axial vs extremities), metastatic event, date of last follow-up, and vital status.

PATHOLOGIC PARAMETERS

In order to provide reproducible criteria to categorize the lesions, only 5 quantitative histological or well-defined parameters were evaluated. The lesion diameter (≤10.0 vs >10.0 mm) was measured on the slide by micrometer. The tumor thickness (≤3.00 vs >3.00 mm) was measured by micrometer according to the method of Breslow.7 Ulceration was defined as an interruption of the whole epidermis, including the stratum corneum. The mitotic rate in the dermal component (0-5, 6-8, or >8/mm2) was recorded after the lesion had been scanned for hot spots.8 The anatomical level (I-IV vs V) was recorded according to the method of Clark et al.9

SCORING SYSTEM

The scoring system was derived from a series of simplified likelihood ratios.10 The scoring system represents a series of rounded ratios between the conditional probabilities for whether each parameter state is associated with metastasis. When the ratio was lower than 1.5, the assigned value was 0.

The 30 patients with sufficient data available to be included in the study included 11 patients with histologically documented metastases and 19 patients without metastasis after a follow-up period of at least 3 years.

Table 2 summarizes the distribution of patients and the ratios of conditional probabilities for each parameter. Among the parameters studied, only age at diagnosis greater than 10 years, diameter of lesion greater than 10.0 mm, presence of ulceration, involvement of the subcutaneous fat (level V), and mitotic activity of at least 6/mm2 carried a ratio of conditional probabilities greater than 1.50 and were therefore used for the grading system.

Table Graphic Jump LocationTable 2. Patient Characteristics and Conditional Probabilities

The grading system is presented in Table 3.

Table Graphic Jump LocationTable 3. Grading System for Atypical Spitz Tumors

The lesions were then graded and categorized. Table 4 summarizes the distribution of cases by category of risk. Among 15 cases categorized as Spitz tumor with low risk of metastasis, only 1 case was characterized by lymph node metastasis and death. The patient was a 15-year-old boy with a lesion on the neck; he died 7 months after diagnosis.6 Histologically, the tumor measured 4.4 mm in diameter and 2.95 mm thick, involved the reticular dermis but not the subcutaneous fat, and displayed a mitotic rate of 5/mm2. The morphologic appearance suggested an atypical Spitz nevus and a halo nevus (Figure 1). Three of 6 cases categorized as intermediate risk and 7 of 9 categorized as high risk (Figure 2) had metastases.

Table Graphic Jump LocationTable 4. Distribution by Risk Category
Place holder to copy figure label and caption
Figure 1.

Atypical Spitz tumor with metastasis and death. Left, The lesion is dome-shaped and symmetrical and measures less than 3 mm in diameter. Right, Cells are typical Spitz nevus cells, containing abundant cytoplasm and large nuclei. Mitotic activity is low (5/mm2).

Graphic Jump Location
Place holder to copy figure label and caption
Figure 2.

Atypical Spitz tumor removed from the lower limb of a 14-year-old boy. An inguinal lymph node metastasis appeared 2 years after diagnosis. Left, The lesion is symmetrical and uniform but measures 12 mm in diameter. Right, The subcutaneous fat contains a tumoral nodule. Mitotic activity is 6/mm2.

Graphic Jump Location

We describe a grading system for the categorization of Spitz tumors in children and adolescents. This scoring system is based on our experience with 30 cases with metastasis and/or follow-up of at least 3 years.

Spitz nevi are defined by a set of histological features that has evolved from the initial description by Sophie Spitz in 1948.11 There is a category of lesions that do not demonstrate the classic features of Spitz nevi or that exhibit atypical features. Since no set of criteria can predict clinical outcome with certainty in this group of lesions, the dichotomous categorization into nevus and melanoma appears artificial. Moreover, the final diagnosis is often based on the degree of deviation of these lesions from the classic Spitz nevus. Therefore, it is not unexpected that the threshold to make a diagnosis of melanoma in the group of atypical Spitz tumors should vary from one pathologist to another and that these lesions constitute one of the most important sources of discordance among pathologists in the field of the melanocytic lesions. We propose the separation of Spitz tumors into 3 groups: unequivocal Spitz tumors without any abnormal or unusual features, melanomas, and atypical Spitz tumors. For the latter category we propose a grading system for the categorization of risk for metastasis as low, intermediate, or high.

There are 2 main justifications for the use of a grading system: to improve on the predictive value of conventional histological analysis and to increase the reproducibility between observers for diagnosis and assessment of prognosis. With respect to Spitz tumors and related lesions, 2 antithetical views are presented in the literature. According to one view, most of the lesions diagnosed as Spitz nevi in reality deviate from the generally accepted criteria and therefore represent a phenotypic continuum between the Spitz nevus and melanoma.12 According to another perspective, the Spitz nevus is a completely benign lesion that has no relation to melanoma biologically and in many cases displays features that permit an unequivocal diagnosis of Spitz nevus.13 The reports of a fatal outcome from lesions not distinguishable from Spitz nevi support the first position.6,1418 It is our view that even though the latter cases are quite rare, their existence justifies the idea that all Spitz tumors have some potential risk for metastasis. Perhaps more frequently encountered are the group of Spitzlike lesions with metastatic evolution, for which no definitive diagnosis of nevus or melanoma could be made a priori. It is likely beyond the scope of routine histopathology to render a definitive diagnosis for these lesions. The problem is illustrated in the present study by the case with metastasis and death, which was diagnosed as a nevus according to the classic dichotomous system. This lesion would have been classified as an atypical Spitz tumor with low risk of metastasis according to our grading system. Several authors have recently suggested that the current histological criteria for diagnosing melanocytic neoplasms are highly prone to variable interpretation and are entirely subjective,19,20 indicating a lack of reliability. These statements are even more applicable to the specific category of Spitz tumors. Consequently, we believe that our grading system should promote better reproducibility among observers for the histological evaluation of Spitz tumors.

The parameters evaluated to establish the grading system were either quantitative or easily definable. Seventy percent of Spitz tumors occur in patients younger than 20 years, and among these, half are diagnosed before age 10 years.21 On the other hand, melanomas are extremely rare in children less than 10 years of age. It is estimated that 94% of Spitz nevi are less than 1 cm in diameter.21 Most of the reported Spitz tumors with metastases measure more than 1 cm. In the present series, fat involvement was observed more frequently in patients with metastatic evolution. Since, as previously reported, tumor thickness is the major prognostic factor in childhood melanoma,2 it is likely that fat involvement is a correlate of tumor thickness, which failed to have prognostic value because of the small series of patients. In most of the comparative studies attempting to identify the most discriminant features for the differential diagnosis of Spitz nevi and melanoma, ulceration was frequently associated with metastasis. Mitoses may be absent, rare, or numerous both in Spitz tumors without metastatic evolution and in fatal melanomas. However, a high dermal mitotic rate was often associated with metastatic evolution. Deeply located mitoses have also been ascribed to melanoma. However, the evaluation of depth of a mitosis is often subjective and related to tumor thickness.

Since the cases in this series were used to establish the grading system, it is not unexpected that there was an increase in the number of patients with metastatic evolution according to grade. Therefore, it is necessary to validate this proposed grading system in an independent database and with a larger number of patients. We strongly believe that the application of an objective grading system such as the one described herein for the first time is the first step in providing useful information for the management of atypical Spitz tumors.

Accepted for publication August 21, 1998.

Corresponding author: Raymond L. Barnhill, MD, Division of Dermatopathology and Oral Pathology, the Johns Hopkins Medical Institutions, 600 N Wolfe St, Baltimore, MD 21287-4915.

Allen  ACSpitz  S Malignant melanoma: a clinicopathological analysis of the criteria for diagnosis and prognosis. Cancer. 1953;61- 45
Spatz  ARuiter  DHardmeier  T  et al.  Melanoma in childhood: an EORTC-MCG multicenter study on the clinico-pathological aspects. Int J Cancer. 1996;68317- 324
Handfield-Jones  SESmith  NP Malignant melanoma in childhood. Br J Dermatol. 1996;134607- 616
Barnhill  RLFlotte  TJFleischli  MPerez-Atayde  A Cutaneous melanoma and atypical Spitz tumors in childhood. Cancer. 1995;761833- 1845
Barnhill  RL Tumors of melanocytes. Textbook of Dermatopathology. New York, NY McGraw-Hill Book Co1998;537- 591
Busam  KJBarnhill  RL Spitz nevi and related lesions. Barnhill  RLed.Pathology of Melanocytic Nevi and Malignant Melanoma. Newton, Mass Butterworth-Heinemann1995;97- 130
Breslow  A Thickness, cross-sectional areas and depth of invasion in the prognosis of cutaneous melanoma. Ann Surg. 1970;172902- 908
Clark  WH  JrElder  DEDupont IV  G  et al.  Model predicting survival in stage I melanoma based on tumor progression. J Natl Cancer Inst. 1989;811893- 1904
Clark  WH  JrFrom  LBernadino  EAMihm  MC The histogenesis and biologic behavior of primary human malignant melanomas of the skin. Cancer Res. 1969;29705- 727
Pera  ABellando  PCaldera  D  et al.  Colonoscopy in inflammatory bowel disease: diagnostic accuracy and proposal of an endoscopic score. Gastroenterology. 1987;92181- 185
Spitz  S Melanomas of childhood. Am J Pathol. 1948;24591- 609
Piepkorn  M On the nature of histologic observations: the case of the Spitz nevus. J Am Acad Dermatol. 1995;32248- 254
Shapiro  PE Spitz nevi [letter]. J Am Acad Dermatol. 1993;29667- 668
Okun  MR Melanoma resembling spindle and epithelioid cell nevus. Arch Dermatol. 1979;1151416- 1420
Smith  KJBarrett  TLSkelton  HGLupton  GPGraham  JH Spindle cell and epitheloid cell nevi with atypia and metastasis (malignant Spitz nevus). Am J Surg Pathol. 1989;13931- 939
Mehregan  AHMehregan  DA Malignant melanoma in childhood. Cancer. 1993;714096- 4103
Goldes  JHolmes  SSatz  M  et al.  Melanoma masquerading as Spitz nevus following acute lymphoblastic leukemia. Pediatr Dermatol. 1984;1295- 298
Casso  EMGrin-Jorgensen  CMGrant-Kels  JM Spitz nevi. J Am Acad Dermatol. 1992;27901- 913
Farmer  ERGonin  RHanna  MP Discordance in the histopathologic diagnosis of melanoma and melanocytic nevi between expert pathologists. Hum Pathol. 1996;27528- 531
Ackerman  AB Discordance among expert pathologists in diagnosis of melanocytic neoplasms. Hum Pathol. 1996;271115- 1116
Weedon  DLittle  JH Spindle and epitheloid cell nevi in children and adults: a review of 211 cases of the Spitz nevus. Cancer. 1977;40217- 225

Figures

Place holder to copy figure label and caption
Figure 1.

Atypical Spitz tumor with metastasis and death. Left, The lesion is dome-shaped and symmetrical and measures less than 3 mm in diameter. Right, Cells are typical Spitz nevus cells, containing abundant cytoplasm and large nuclei. Mitotic activity is low (5/mm2).

Graphic Jump Location
Place holder to copy figure label and caption
Figure 2.

Atypical Spitz tumor removed from the lower limb of a 14-year-old boy. An inguinal lymph node metastasis appeared 2 years after diagnosis. Left, The lesion is symmetrical and uniform but measures 12 mm in diameter. Right, The subcutaneous fat contains a tumoral nodule. Mitotic activity is 6/mm2.

Graphic Jump Location

Tables

Table Graphic Jump LocationTable 1. Comparison of Classic Spitz Nevi and Atypical Spitz Tumors*
Table Graphic Jump LocationTable 2. Patient Characteristics and Conditional Probabilities
Table Graphic Jump LocationTable 3. Grading System for Atypical Spitz Tumors
Table Graphic Jump LocationTable 4. Distribution by Risk Category

References

Allen  ACSpitz  S Malignant melanoma: a clinicopathological analysis of the criteria for diagnosis and prognosis. Cancer. 1953;61- 45
Spatz  ARuiter  DHardmeier  T  et al.  Melanoma in childhood: an EORTC-MCG multicenter study on the clinico-pathological aspects. Int J Cancer. 1996;68317- 324
Handfield-Jones  SESmith  NP Malignant melanoma in childhood. Br J Dermatol. 1996;134607- 616
Barnhill  RLFlotte  TJFleischli  MPerez-Atayde  A Cutaneous melanoma and atypical Spitz tumors in childhood. Cancer. 1995;761833- 1845
Barnhill  RL Tumors of melanocytes. Textbook of Dermatopathology. New York, NY McGraw-Hill Book Co1998;537- 591
Busam  KJBarnhill  RL Spitz nevi and related lesions. Barnhill  RLed.Pathology of Melanocytic Nevi and Malignant Melanoma. Newton, Mass Butterworth-Heinemann1995;97- 130
Breslow  A Thickness, cross-sectional areas and depth of invasion in the prognosis of cutaneous melanoma. Ann Surg. 1970;172902- 908
Clark  WH  JrElder  DEDupont IV  G  et al.  Model predicting survival in stage I melanoma based on tumor progression. J Natl Cancer Inst. 1989;811893- 1904
Clark  WH  JrFrom  LBernadino  EAMihm  MC The histogenesis and biologic behavior of primary human malignant melanomas of the skin. Cancer Res. 1969;29705- 727
Pera  ABellando  PCaldera  D  et al.  Colonoscopy in inflammatory bowel disease: diagnostic accuracy and proposal of an endoscopic score. Gastroenterology. 1987;92181- 185
Spitz  S Melanomas of childhood. Am J Pathol. 1948;24591- 609
Piepkorn  M On the nature of histologic observations: the case of the Spitz nevus. J Am Acad Dermatol. 1995;32248- 254
Shapiro  PE Spitz nevi [letter]. J Am Acad Dermatol. 1993;29667- 668
Okun  MR Melanoma resembling spindle and epithelioid cell nevus. Arch Dermatol. 1979;1151416- 1420
Smith  KJBarrett  TLSkelton  HGLupton  GPGraham  JH Spindle cell and epitheloid cell nevi with atypia and metastasis (malignant Spitz nevus). Am J Surg Pathol. 1989;13931- 939
Mehregan  AHMehregan  DA Malignant melanoma in childhood. Cancer. 1993;714096- 4103
Goldes  JHolmes  SSatz  M  et al.  Melanoma masquerading as Spitz nevus following acute lymphoblastic leukemia. Pediatr Dermatol. 1984;1295- 298
Casso  EMGrin-Jorgensen  CMGrant-Kels  JM Spitz nevi. J Am Acad Dermatol. 1992;27901- 913
Farmer  ERGonin  RHanna  MP Discordance in the histopathologic diagnosis of melanoma and melanocytic nevi between expert pathologists. Hum Pathol. 1996;27528- 531
Ackerman  AB Discordance among expert pathologists in diagnosis of melanocytic neoplasms. Hum Pathol. 1996;271115- 1116
Weedon  DLittle  JH Spindle and epitheloid cell nevi in children and adults: a review of 211 cases of the Spitz nevus. Cancer. 1977;40217- 225

Correspondence

CME
Meets CME requirements for:
Browse CME for all U.S. States
Accreditation Information
The American Medical Association is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. The AMA designates this journal-based CME activity for a maximum of 1 AMA PRA Category 1 CreditTM per course. Physicians should claim only the credit commensurate with the extent of their participation in the activity. Physicians who complete the CME course and score at least 80% correct on the quiz are eligible for AMA PRA Category 1 CreditTM.
Note: You must get at least of the answers correct to pass this quiz.
You have not filled in all the answers to complete this quiz
The following questions were not answered:
Sorry, you have unsuccessfully completed this CME quiz with a score of
The following questions were not answered correctly:
Commitment to Change (optional):
Indicate what change(s) you will implement in your practice, if any, based on this CME course.
Your quiz results:
The filled radio buttons indicate your responses. The preferred responses are highlighted
For CME Course: A Proposed Model for Initial Assessment and Management of Acute Heart Failure Syndromes
Indicate what changes(s) you will implement in your practice, if any, based on this CME course.
NOTE:
Citing articles are presented as examples only. In non-demo SCM6 implementation, integration with CrossRef’s "Cited By" API will populate this tab (http://www.crossref.org/citedby.html).
Submit a Comment

Multimedia

Some tools below are only available to our subscribers or users with an online account.

Web of Science® Times Cited: 92

Related Content

Customize your page view by dragging & repositioning the boxes below.

Articles Related By Topic
Related Topics
PubMed Articles